A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047460



Internal ID21956693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108689608..108689608hg38UCSC Ensembl
chr1:109232230..109232230hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer